FDA UDI Not in Commercial Distribution 🇺🇸 United States

FMS

DI: 10886705023769 · Model: 218022 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FMS
Primary DI
10886705023769
Version / Model
218022
Catalog Number
218022
Company Name
DEPUY MITEK, LLC
Labeler DUNS
190572854
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-30
Public Version
6
Public Version Date
2021-01-28
Public Version Status
Update
Public Device Record Key
b63e219e-42aa-4f99-b09d-7b81b7c583b7
Distribution End Date
2021-01-28

Device Description

FMS INFLOW/OUTFLOW SHEATH KIT Inflow/Outflow-Linvatec

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
37086 Endoscope sheath, reusable

Identifiers

Type ID
Primary 10886705023769

Customer Contacts